- Andropause, Anti Aging-HGH, Anti Aging-Stem Cells, Anti Aging Gene Therapy, Bone Loss Molecular Therapy, Fibromyalgia Molecular Therapy, Herpes Zoster Gene Therapy, Human Vomeronasal Stimulation, Influenza Molecular Therapy, Injury Recovery Molecular Therapy, Melanoma Gene Therapy, Menopause, Muscle Wastage Gene Therapy, N-Glycolylneuraminic Acid Stimulation, Nerve Regeneration Molecular Therapy, Olfactory Receptors Stimulation, Physical Endurance Profile Gene Therapy, Rheumatoid Arthritis Molecular Therapy, Secondary Lymphedema Gene Therapy, UV Protection, Urate Oxidase Stimulation, Molecular Biology, Biotechnology, Bioengineering, Genetic Therapies, Alternative Medicine, Alternative Therapies, Resonant Therapy, Therapy, Healing Remedies, Vibrational Therapies, Healing Sound, Music-Sound Frequencies Mix, Public Domain, ok33
correspond either to the molar mass or equivalent scalar
octave of the related products.
This work is dedicated to the public domain and
may be reproduced without authorization.
* Andropause, addresses common manopause issues such as osteoarthritis,
arthritis rheumatoid, enlarged prostate, knee problems, graying hair or
diabetes. Immunosuppressants, omega 3 acids, superoxide dismutases,
antioxidants and sex hormone-binding globulin (SHBG). Unless stated otherwise
each item plays for 3m.
Left channel: Golimumab, Etanercept, Certolizumab pegol, SOD 1, SOD 3, SOD 2,
DHA, AA, EPA, ALA.
Right channel: SHBG glycoprotein (6m), Catalase, 3,4-Divanillyltetrahydrofuran
(6m), SDA, Alpha Lipoic acid, Indole-3-Carbinol (6m), Zinc.
* Anti aging HGH, a focus on the endocrine hormone produced by the pituitary
gland and insuline activation by IGF-1. Decreasing levels of HGH raise risks of
body fat, bone fragility, weak/wrinkled skin, reduced energy, and loss of
memory. Unless stated otherwise each item plays for 3m.
Left channel: Phosphatidylinositol, GHRH, Ibutamoren, Capromorelin,
Macimorelin, HGH, CJC-1295, Somatrem, GABA, Lysine, Ornithine (2m).
Right channel: IGF-1, Protopanaxatriol, Protopanaxadiol, Stigmastanol,
beta-Sitosterol, Stigmasterol, Phosphatidylserine, Tryptophan, Arginine,
Glutamine, Glycine (2m).
* Anti aging stem cells, six factor approach to reprogram senescent cells into
induced pluripotent stem cells (iPSC's). Gene factors used, according to
INSERM's AVENIR "Genomic plasticity and aging" team, are KLF4, MYC, NANOG,
SOX2, LIN28 and OCT4.
* Anti aging gene therapy, targets shortening of telomeres which protect the
end of the chromosomes from deterioration or from fusion with neighboring
chromosomes. It also provides support for mitochondrial function and regulation
of genes that affect energy metabolism. Unless stated otherwise each item
plays for 4m.
Left channel: SIRT1 protein, Astragaloside, PPARGC1A protein (8m), Glutathione,
DHEA, Genistein, Sulforaphane.
Right channel: PPARGC1A protein, Cycloastragenol, SRT1720, LMNA protein,
5a-Androstane-3b,17b-diol, Daidzein, Resveratrol, Selenium.
* Bone loss molecular therapy, a mix of bisphosphonates, monoclonal antibodies,
an alkaline phosphatase inhibitor, a dual action antiosteoporitic agent, and
gene encoded proteins for bone loss and diseases of bone metabolism.
Romosozumab, Blosozumab, Denosumab, BMP7, Osteoprogeterin, BMP2, Teriparatide,
Strontium Ranelate, Zoledronic Acid, and Homoarginine.
* Fibromyalgia molecular therapy, plays antiemetic drugs and serotonin 5-HT 3
receptor antagonists, a melatonin receptor agonist, a tricyclic muscle
relaxant, a serotonin–norepinephrine reuptake inhibitor (antidepressant and
pain treatment), a prodrug to the neurotransmitters norepinephrine
(noradrenaline) and epinephrine (adrenaline), an anticonvulsant, kappa-opioid
receptor (KOR) and delta-opioid receptor (DOR). Unless stated otherwise each
item plays for 3 minutes. Sequence: KOR (2m), DOR (2m), Azasetron, Tropisetron
hydrochloride, Piromelatine, Tropisetron, Cyclobenzaprine, Milnacipran,
Droxidropa, Pregabalin, KOR (2m), DOR (2m).
* Herpes zoster gene therapy, includes antiviral, symptom management and
postherpetic neuralgia agents. Each item plays for 2m. In playing order, Botox,
Fasinumab, Alefacept, Immune system normalization frequency, Astaxanthin,
Substance P, NGF precursor, Opipramol, Prednisone, Docosanol, Famciclovir,
Capsaicin, Foscarnet, Caladryl, Vidarabine, Tromantadine, Taribavirin, Cidovir,
Lidocaine, Morxydine, Sodium Bromide.
* Human vomeronasal stimulation targets type 1 receptors of the vomeronasal
organ. These receptors are thought to be responsible for pheromone detection.
The frequencies for the receptors VN1R1, VN1R2, VN1R3, VN1R4, and VN1R5 are
included. Some of them appear to be functionless. (See notes below for
* Influenza molecular therapy, frequencies for viral replication, neuraminidase
and M2 protein inhibiton, immune system stimulation, antivirals, and
symptomatic relief. Unless stated otherwise each item plays for 3m.
Left channel: Bavituximab, Diridavumab, Interferon alpha-2b, Arbidol,
Lactoferrin, Anoro Ellipta, Oseltamivir, Zanimivir, Peramivir, Rimantadine,
Right channel: Vitamin B12, Folic acid, Tocopherol, Calcitriol, Vitamin B6,
Elenolic acid, Tymazoline, Ascorbic acid, Pseudoephedrine, Acetylcysteine,
* Injury recovery and range of motion molecular therapy. Each item plays for 3m.
Left channel: MMP8, Serrapeptase, Pancreatin, MMP1, SDHC, Decorin, Nattokinase,
Papain, SMAD3, Rutin.
Right channel: Chymotrypsin C, MMP9, Chymotrypsin A, Iduronidase, PEPCK
cytosolic, SLC22A4, Bromelain, Trypsin, Mannose-6-phosphate, Ergothioneine.
* Melanoma gene therapy, including metastatic melanoma. In playing order,
Pembrolizumab, Peginterferon alpha-2b, Interferon alpha-2b, Proleukin,
Phosphatase and tensin homolog (PTEN), Tremelimumab, Melanocortin 1 receptor
(MC1R), Trametinib, Afamelanotide, BMS-470,539, Dabrafenib, Vemurafenib,
Recombinant interferon alpha-2b, Ipilimumab, Rasagiline.
* Menopause, for women of age and also used for males with fertility, libido or
sexual dysfunction issues. Unless stated otherwise each item plays for 3m.
Left channel: Human chorionic gonadotropin (hCG) beta, Luteinizing hormone (LH),
Follitropin subunit beta (FSHB), hCG alpha, Recombinant hCG, Estrogen receptor 1
(ESR1), Calcitriol, Urofollitropin, Beta sitosterol, Stigmasterol (2m), ESR2
Right channel: UK-414,495, Progesterone, Levonorgestrel, Ellagic acid,
Estradiol, Genistein, Daidzein, Alendronate, Equol (2m), PF-219,061 (2m).
* Muscle wastage gene therapy is conceived to counter aging related loss of
muscle mass. The strategy employed involves myostatin, NF-kB signaling and TNF
inhibition; insulin-like growth factor replacement, nNOS pathway enhancement,
TGF-beta regulation, and anti-oxidants. Unless stated otherwise each item plays
Left channel: Etanercept, Stamulumab (6m), Thymosin beta-4, HSP90B1, Taladafil,
ACVR2B (6m), Mecasermin, Nitroflurbiprofen, Formosterol (2m).
Right channel: Coenzyme Q10, Cobalamin, Epigallocatechin-3-gallate, Curcumin,
Carnitine, Ornithine, Leucine, Creatine, Valine, Proline, Serine (2m).
* N-Glycolylneuraminic acid (Neu5Gc) stimulation translates the molar weight of
this sialic acid molecule into Hz. Humans cannot synthesize it due to
manipulation in the past of the gene CMAH. The recording includes as well the
the translation into Hz of the Neu5Gc based monoclonal antibody Racotumomab. It
is a therapeutic cancer vaccine for the treatment of solid tumors. (See notes
below for pseudogene rationale)
* Nerve regeneration molecular therapy, for neuropathies in general, expresses
gangliosides, aceyl-L-carnitine, neurotrophins, nerve growth factors,
erythropoietin and Fasinumab. The sequence plays in this order Fasinumab, EPO
recombinant, GT1b, GD's (1a, 1b, 2, 3), NGF beta recombinant, GM's (1, 2, 3),
Neurotrophin-3, NGF, bNGF recombinant, NGF beta, NGF beta recombinant, NTF4, EPO
recombinant, EPO, Acetyl-L-carnitine.
* Olfactory receptors stimulation. The Olfactory Receptors (OR) included are
OR2T2P, OR10T1P, OR10R1P, OR10R3P, OR2W3P. (See notes below for pseudogene
Muscle hypertrophy (-) Myostatin inhibitor ACVR2B = 388.941 Hz
Raised muscle glycogen (+) Glyc Synthase GYS1 = 564.546 Hz
Higher haematocrit (+) EPO = 390.252 Hz
Fibre type and mitochondria biogenesis (+), for endurance running (-) PPAR-gamma = 388.239 Hz
Fibre type (-) ACTN3 1-576 = 447.837 Hz
Fibre type and mitochondria biogenesis (+) PGC-1alpha or PPARGC1A = 613.278 Hz
Myocardial hypertrophy (+) MEK1 or MAP2K1 = 795.612 Hz
Endurance running (+) PEPCK1 cytosolic = 466.197 Hz
Fibre type (+) MAPK12 = 768.135 Hz
Longer legs (+) GH or GH-1 = 455.024 Hz
Fibre type (+) Ras AGTR2 = 754.311 Hz
Fibre type (+) Calcineurins PPP3CA = 395.391 Hz, PPP3CB = 398.322 Hz, PPP3CC = 399.330 Hz
Myocardial hypertrophy (+) PI3K = 837.492 Hz
Muscle hypertrophy (+) IGF1 = 848.307 Hz
Muscle hypertrophy (-) PKB inhibitor MK-2206 = 407.478 Hz
(+)(-) refers to turning up or down gene' expression
* Rheumatoid arthritis molecular therapy features monoclonal antibodies to
inhibit tumor necrosis factor-alpha and interleukin-6 receptors. The goal is to
reduce excessive immune reactions. Unless stated otherwise each item plays for
Left channel: Curcumin/Piperine/Quercetin (2m), Golimumab, Tocilizumab,
Adalimumab, Etanercept, Certolizumab pegol.
Right channel: Curcumin/Piperine/Quercetin (2m), Stigmastanol, Glucosamine,
Taurine, Niacin, MSM.
* Secondary lymphedema gene therapy, presents gene factors triggered during a
2013 study by Miaskowski et al. where genetic regression analysis found four
genes (lymphocyte cytosolic protein2- LCP2, neuropilin2-NRP2, protein tyrosine
kinase-SYK, and vascular adhesion molecule1-VCAM1) and 3 haplotypes (forkhead
box protein C2- FOXC2, neuropilin2-NRP2, and vascular endothelial growth factor
C-VEGFC) associated with secondary lymphedema. Each item plays for 5m, in
order, FOXC2, VEGFC, NRP2, VCAM1, SYK, LCP2.
* UV protection, based on a study by Foley, L. E. et al. Human cryptochrome
exhibits light-dependent magnetosensitivity (2011). The recording expresses
both human cryptochromes CRY1 and CRY2 along with omega 3's and other
substances used for UV protection. Each item plays for one minute unless stated
otherwise. The sequence in order, Hearth Chakra body and energy tuner (1m 40s),
Astaxanthin, Prodelphinidin B3, Lutein, Lycopene, Epigallocatechin gallate,
CRY1 (2m), CRY2 (2m), 6',7'-Dihydroxybergamottin, Bergamoitin, DHA,
Gallocatechol, AA, EPA, Ellagic acid, Auraptene, Catechin, Fisetin, ALA, SDA,
Resveratrol, Bergapten, Bergaptol, Sulforaphane.
* Urate oxidase stimulation, UO is an enzyme that catalyzes the oxidation of
uric acid to allantoin in most mammals, but not in humans. Rasburicase and
another recombinant human version of the enzyme are included. (See notes below
for pseudogene rationale)
Algorithmic piano music mixed with sound frequencies.
AIRL ON MOLECULAR BIOLOGY
"The text of books I have been given on subjects related to the function of life forms contain information that is based on false memories, inaccurate observation, missing data, unproven theories, and superstition.
In addition to the application of incorrect theories concerning biological engineering, many primary errors that Earth scientists make are the result of an ignorance of the nature and relative importance of IS-BEs* as the source of energy and intelligence which animate every life form.
It should be noted that much of the "Old Testament" was written during the captivity of the Jews who were enslaved in Babylon, which was very heavily controlled by priests of the "Old Empire". The book introduces a false sense of time and a false concept of the origin of the creation.
The theory of evolution assumes that the motivational source of energy that animates every life form does not exist. It assumes that an inanimate object or a chemical concoction can suddenly become "alive" or animate accidentally or spontaneously.
No Western scientist ever stopped to consider who, what, where, when or how this animation happens. Complete ignorance, denial or unawareness of the spirit as the source of life force required to animate inanimate objects or cellular tissue is the sole cause of failures in Western medicine.
In addition, evolution does not occur accidentally. It requires a great deal of technology which must be manipulated under the careful supervision of IS-BEs. Very simple examples are seen in the modification of farm animals or in the breeding of dogs. However, the notion that human biological organisms evolved naturally from earlier ape-like forms is incorrect. No physical evidence will ever be uncovered to substantiate the notion that modern humanoid bodies evolved on this planet.
The reason is simple: the idea that human bodies evolved spontaneously from the primordial ooze of chemical interactivity in the dim mists of time is nothing more than a hypnotic lie instilled by the amnesia operation to prevent your recollection of the true origins of Mankind. Factually, humanoid bodies have existed in various forms throughout the universe for trillions of years.
Biological bodies on most "Sun Type 12, Class 7" planets are usually engineered to last for an average of about 150 years. Human bodies on Earth last only about one half as long. We suspect this is because the prison administrators have altered the biological material of human bodies on Earth to die more frequently so that the IS-BEs who inhabit them will recycle through the amnesia mechanism more frequently." (Excerpts from Alien Interview)
* Immortal Spiritual Beings
- 2014-03-09 14:28:56.00227
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